Multi-Institutional Data Collection and Analysis via the Pediatric Proton/Photon Consortium Registry

N. Denunzio, M. Lawell, T. Yock
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Abstract

Care of patients with proton therapy has increased in the past decade. It is important to report on outcomes and disease specific utilization of particle therapy. In this chapter, we review our experience in developing a registry for pediatric patients treated with radiation to assess outcomes and provide a platform for shared research interests.
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通过儿科质子/光子联盟注册的多机构数据收集和分析
在过去的十年中,对质子治疗患者的护理有所增加。报道颗粒治疗的结果和疾病特异性应用是很重要的。在本章中,我们回顾了我们在为接受放射治疗的儿科患者建立注册表方面的经验,以评估结果,并为共享研究兴趣提供一个平台。
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Proton Therapy in Lower-Middle-Income Countries: From Facts and Reality to Desire, Challenges and Limitations History and Overview of Proton Therapy Proton Therapy Center Layout and Interface The Future of Proton Therapy Multi-Institutional Data Collection and Analysis via the Pediatric Proton/Photon Consortium Registry
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